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au.\*:("SPRANGER JW")

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METAPHYSEAL CHONDRODYSPLASIA.SPRANGER JW.1977; POSTGRAD. MED. J.; G.B.; DA. 1977; VOL. 53; NO 622; PP. 480-487; BIBL. 1 P.; (BONE DYSPLASIAS. SYMP. PROC.; BRISTOL; 1976)Conference Paper

CATABOLIC DISORDERS OF COMPLEX CARBOHYDRATES.SPRANGER JW.1977; POSTGRAD. MED. J.; G.B.; DA. 1977; VOL. 53; NO 622; PP. 441-449; BIBL. 6 REF.; (BONE DYSPLASIAS. SYMP. PROC.; BRISTOL; 1976)Conference Paper

KNIEST DISEASESPRANGER JW; MAROTEAUX P.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 12; PP. 50-56; BIBL. 4REF.Article

CAMPOMELIC DYSPLASIA: FURTHER ELUCIDATION OF A DISTINCT ENTITYHALL BD; SPRANGER JW.1980; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1980; VOL. 134; NO 3; PP. 285-289; BIBL. 28 REF.Article

FAMILIAL CONGENITAL BOWING WITH SHORT BONESHALL BD; SPRANGER JW.1979; RADIOLOGY; USA; DA. 1979; VOL. 132; NO 3; PP. 611-614; BIBL. 5 REF.Article

EDITORIAL COMMENT: GENETIC HETEROGENEITY OF SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA.SPRANGER JW; MAROTEAUX P.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 3; PP. 241-242; BIBL. 4 REF.Article

DEVELOPMENTAL TERMS-SOME PROPOSALS: FIRST REPORT OF AN INTERNATIONAL WORKING GROUPBENIRSCHKE K; LOWRY RB; OPITZ JM et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 3; PP. 297-302; BIBL. 21 REF.Article

THE STICKLER SYNDROME (HEREDITARY ARTHROOPHTHALMOPATHY) = LE SYNDROME DE STICKLER, ARTHRO-OPHTALMOPATHIE HEREDITAIREHERRMANN J; FRANCE TD; SPRANGER JW et al.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 76-103; BIBL. 38 REF.Article

PATHOLOGY OF CHONDRODYSPLASIA PUNCTATA RHIZOMELIC TYPEVISESKUL C; OPITZ JM; SPRANGER JW et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 12; PP. 327-333; BIBL. 2REF.Article

CEREBROARTHRODIGITAL SYNDROME: A NEWLY RECOGNIZED FORMAL GENESIS SYNDROME IN THREE PATIENTS WITH APPARENT ARTHROMYODYSPLASIA AND SACRAL AGENESIS, BRAIN MALFORMATION AND DIGITAL HYPOPLASIASPRANGER JW; SCHINZEL A; MYERS T et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 1; PP. 13-24; BIBL. 39 REF.Article

THE CAMPOMELIC SYNDROME: REVIEW, REPORT OF 17 CASES, AND FOLLOW-UP ON THE CURRENTLY 17-YEAR-OLD BOY FIRST REPORTED BY MAROTEAUX ET AL. IN 1971HOUSTON CS; OPITZ JM; SPRANGER JW et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 3-28; BIBL. 4 P.Article

GREBE CHONDRODYSPLASIA AND SIMILAR FORMS OF SEVERE SHORT-LIMBED DWARFISM.ROMEO G; ZONANA J; LACHMAN RS et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3C; PP. 109-115; BIBL. 10 REF.Article

STUDIES OF MALFORMATION SYNDROMES OF MAN XIB: THE CEREBRO-HEPATO-RENAL SYNDROME OF ZELLWEGER: COMPARATIVE PATHOLOGY = ETUDES SUR LES SYNDROMES MALFORMATIFS DE L'HOMME XIB: LE SYNDROME CEREBRO-HEPATO-RENAL DE ZELLWEGER: ANATOMIE PATHOLOGIQUE COMPAREEGILCHRIST KW; GILBERT F; GOLDFARB S et al.1976; EUROP. J. PEDIATR.; GERM.; DA. 1976; VOL. 121; NO 2; PP. 99-118; BIBL. 1 P. 1/2Article

THE W SYNDROME. STUDIES OF MALFORMATION SYNDROMES OF MAN. XXVIII.PALLISTER PD; HERRMANN J; SPRANGER JW et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 51-60; BIBL. 3 REF.Article

CHONDRODYSPLAZIA PUNCTATA-RHIZOMELIC FORM-PATHOLOGIC AND RADIOLOGIC STUDIES OF THREE INFANTS.GILBERT EF; OPITZ JM; SPRANGER JW et al.1976; EUROP. J. PEDIATR.; GERM.; DA. 1976; VOL. 123; NO 2; PP. 89-109; BIBL. 1 P. 1/2Article

HETEROGENEITY OF NONLETHAL SEVERE SHORT-LIMBED DWARFISM.ROMEO G; ZONANA J; RIMOIN DL et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 91; NO 6; PP. 918-923; BIBL. 17 REF.Article

JUVENILE GM1 GANGLIOSIDOSIS: CLINICAL, PATHOLOGICAL, CHEMICAL AND ENZYMATIC STUDIES = GANGLIOSIDOSE GM1 JUVENILE: ETUDE CLINIQUE, ANATOMO-PATHOLOGIQUE, CHIMIQUE ET ENZYMATIQUEO'BRIEN JS; HO MW; VEATH ML et al.1972; CLIN. GENET.; DANM.; DA. 1972; VOL. 3; NO 6; PP. 411-434; BIBL. 22REF.Serial Issue

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